Shantel Weinsheimer, PhD

Title(s)Assistant Professor, Anesthesia
SchoolSchool of Medicine
Address521 Parnassus Avenue, #4515
San Francisco CA 94117
Phone628-206-8908
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    Collapse Biography 
    Collapse Education and Training
    Wayne State University, Detroit, MIPhD08/2006Molecular Biology & Genetics
    Wayne State University, Detroit, MIMS06/2002Basic Medical Sciences
    Otterbein College, Westerville, OHBS06/1999Biochemistry and Life Science

    Collapse Overview 
    Collapse Overview
    Dr. Weinsheimer’s research interests include human genetics studies of cerebrovascular malformations and neuropsychiatric disorders. Her group’s main focus is the identification of clinical genomics tools (e.g., genetic, epigenetic, transcriptomic, or microbiome biomarkers) that can aid early detection, stratify patient subtypes and result in improved clinical management for individuals with brain vascular malformations including brain AVM, aneurysm, Cerebral Cavernous Malformation and Hereditary Hemorrhagic Telangiectasia. Current approaches include genome-wide association studies, screening for rare variants, investigation of somatic variation, and blood expression profiling to identify molecular markers of poor outcome (e.g. hemorrhage).

    Institute for Human Genetics - Faculty Member
    Center for Cerebrovascular Research - Faculty Member

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation. J Am Heart Assoc. 2023 02 07; 12(3):e027572. Weinsheimer S, Nelson J, Abla AA, Ko NU, Tsang C, Okoye O, Zabramski JM, Akers A, Zafar A, Mabray MC, Hart BL, Morrison L, McCulloch CE, Kim H, Brain Vascular Malformation Consortium Cerebral Cavernous Malformation Investigator Group *. PMID: 36695309; PMCID: PMC9973654.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. A single-cell atlas of the normal and malformed human brain vasculature. Science. 2022 03 04; 375(6584):eabi7377. Winkler EA, Kim CN, Ross JM, Garcia JH, Gil E, Oh I, Chen LQ, Wu D, Catapano JS, Raygor K, Narsinh K, Kim H, Weinsheimer S, Cooke DL, Walcott BP, Lawton MT, Gupta N, Zlokovic BV, Chang EF, Abla AA, Lim DA, Nowakowski TJ. PMID: 35084939; PMCID: PMC8995178.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    3. Endoluminal Biopsy for Molecular Profiling of Human Brain Vascular Malformations. Neurology. 2022 04 19; 98(16):e1637-e1647. Winkler E, Wu D, Gil E, McCoy D, Narsinh K, Sun Z, Mueller K, Ross J, Kim H, Weinsheimer S, Berger M, Nowakowski T, Lim D, Abla A, Cooke D. PMID: 35145012; PMCID: PMC9052570.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    4. Abstract 109: Biological Pathways Enriched For Genes Associated With Lesion Burden In Cerebral Cavernous Malformation. Stroke. 2022 Feb 1; 53(Suppl_1):a109-a109. Sriram SA, Weinsheimer WS, Nelson NJ, Mabray MM, Zabramski ZJ, Akers AA, Hart HB, Morrison ML, McCulloch MC, Kim KH. .
      View in: Publisher Site   Mentions:
    5. Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet J Rare Dis. 2021 09 19; 16(1):390. Thompson KP, Nelson J, Kim H, Weinsheimer SM, Marchuk DA, Lawton MT, Krings T, Faughnan ME, Brain Vascular Malformation Consortium HHT Investigator Group. PMID: 34538258; PMCID: PMC8451134.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation. Mol Genet Genomic Med. 2021 10; 9(10):e1794. Choksi F, Weinsheimer S, Nelson J, Pawlikowska L, Fox CK, Zafar A, Mabray MC, Zabramski J, Akers A, Hart BL, Morrison L, McCulloch CE, Kim H. PMID: 34491620; PMCID: PMC8580075.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    7. Pilot investigation of circulating angiogenic and inflammatory biomarkers associated with vascular malformations. Orphanet J Rare Dis. 2021 09 03; 16(1):372. Wetzel-Strong SE, Weinsheimer S, Nelson J, Pawlikowska L, Clark D, Starr MD, Liu Y, Kim H, Faughnan ME, Nixon AB, Marchuk DA. PMID: 34479577; PMCID: PMC8414780.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    8. Seizure Incidence Rates in Children and Adults With Familial Cerebral Cavernous Malformations. Neurology. 2021 Aug 13. Fox CK, Nelson J, McCulloch CE, Weinsheimer S, Pawlikowska L, Hart B, Mabray M, Zafar A, Morrison L, Zabramski JM, Akers A, Kim H. PMID: 34389651; PMCID: PMC8480481.
      View in: PubMed   Mentions: 4     Fields:    
    9. Somatic mosaicism in the MAPK pathway in sporadic brain arteriovenous malformation and association with phenotype. J Neurosurg. 2022 01 01; 136(1):148-155. Gao S, Nelson J, Weinsheimer S, Winkler EA, Rutledge C, Abla AA, Gupta N, Shieh JT, Cooke DL, Hetts SW, Tihan T, Hess CP, Ko N, Walcott BP, McCulloch CE, Lawton MT, Su H, Pawlikowska L, Kim H. PMID: 34214981; PMCID: PMC8720328.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    10. Review of treatment and therapeutic targets in brain arteriovenous malformation. J Cereb Blood Flow Metab. 2021 12; 41(12):3141-3156. Pan P, Weinsheimer S, Cooke D, Winkler E, Abla A, Kim H, Su H. PMID: 34162280; PMCID: PMC8669284.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansAnimalsCells
    11. Abstract MP11: Circulating Plasma Biomarkers Associated With Brain Arteriovenous Malformations. Stroke. 2021 Mar 1; 52(Suppl_1). Wetzel-Strong WS, Weinsheimer WS, Nelson NJ, Pawlikowska PL, Clark CD, McCulloch MC, Kim KH, Faughnan FM, Marchuk MD. .
      View in: Publisher Site   Mentions:
    12. Abstract P42: Genetic Variants Associated With Vasospasm Following Aneurysmal Subarachnoid Hemorrhage. Stroke. 2021 Mar 1; 52(Suppl_1). Weinsheimer WS, Alexander AM, Nelson NJ, Cooke CD, Hetts HS, McCulloch MC, Kim KH, Ko KN. .
      View in: Publisher Site   Mentions:
    13. Maternal and Fetal Outcomes in Women with Brain Arteriovenous Malformation Rupture during Pregnancy. Cerebrovasc Dis. 2021; 50(3):296-302. Yan KL, Ko NU, Hetts SW, Weinsheimer S, Abla AA, Lawton MT, Kim H. PMID: 33640891; PMCID: PMC8159887.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    14. 47 TRYGGVE2: PREDICTING POOR OUTCOMES IN SCHIZOPHRENIA USING REGISTER GENOMICS IN SWEDEN. European Neuropsychopharmacology. 2019 Oct 1; 29:s85-s86. Kowalec KK, Yi YL, Drange DO, Weinsheimer WS, Tesli TM, Folkersen FL, Werge WT, Andreassen AO, Reichborn-Kjennerud RT, Sullivan SP. .
      View in: Publisher Site   Mentions:
    15. 23 SEX CHROMOSOME ANEUPLOIDIES ARE UNDERDIAGNOSED AND INCREASE RISK FOR MENTAL DISORDERS. European Neuropsychopharmacology. 2019 Oct 1; 29:s71-s72. Sanchez SX, Werge WT, Ingason IA, Weinsheimer WS. .
      View in: Publisher Site   Mentions:
    16. M33 TRYGGVE2: PREDICTING POOR OUTCOMES IN MAJOR DEPRESSION USING REGISTER GENOMICS IN SWEDEN. European Neuropsychopharmacology. 2019 Oct 1; 29:s183-s184. Lu LY, Kowalec KK, Drange DO, Tesli TM, Weinsheimer WS, Folkersen FL, Werge WT, Andreassen AO, Reichborn-Kjennerud RT, Sullivan SP. .
      View in: Publisher Site   Mentions:
    17. 26 ESTIMATED DNA METHYLATION GESTATIONAL AGE IN NEWBORN MONOZYGOTIC TWINS ASSOCIATE WITH LATER PSYCHIATRIC DISORDERS BETWEEN CON/DISCORDANT PAIRS. European Neuropsychopharmacology. 2019 Jan 1; 29:s795. Hansen HC, Drong DA, Starnawska SA, Bybjerg-Grauholm BJ, Buil BA, Weinsheimer WS, Bækvad-Hansen BM, Hougaard HD, Lindgren LC, Werge WT. .
      View in: Publisher Site   Mentions:
    18. SU56 DIFFERENTIAL DNA METHYLATION AT BIRTH ASSOCIATED WITH MENTAL DISORDER IN INDIVIDUALS WITH 22Q11.2 DELETION SYNDROME. European Neuropsychopharmacology. 2019 Jan 1; 29:s918. Starnawska SA, Hansen HC, Sparsø ST, Mazin MW, Olsen OL, Bertalan BM, Buil BA, Bybjerg-Grauholm BJ, Bækvad-Hansen BM, Hougaard HD, Mortensen MP, Pedersen PC, Nyegaard NM, Werge WT, Weinsheimer WS. .
      View in: Publisher Site   Mentions:
    19. 25 GENOME-WIDE METHYLOMIC ANALYSIS OF NEONATAL BLOOD FROM DANISH TWINS DISCORDANT FOR MENTAL ILLNESS. European Neuropsychopharmacology. 2019 Jan 1; 29:s794-s795. Weinsheimer WS, Starnawska SA, Hansen HC, Buil BA, Bybjerg-Grauholm BJ, Bækvad-Hansen BM, Hougaard HD, Sparsø ST, Bertalan BM, Mortensen MP, Pedersen PC, Werge WT. .
      View in: Publisher Site   Mentions:
    20. Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study. Lancet Psychiatry. 2018 07; 5(7):573-580. Olsen L, Sparsø T, Weinsheimer SM, Dos Santos MBQ, Mazin W, Rosengren A, Sanchez XC, Hoeffding LK, Schmock H, Baekvad-Hansen M, Bybjerg-Grauholm J, Daly MJ, Neale BM, Pedersen MG, Agerbo E, Mors O, Børglum A, Nordentoft M, Hougaard DM, Mortensen PB, Geschwind DH, Pedersen C, Thompson WK, Werge T. PMID: 29886042; PMCID: PMC6560180.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansCells
    21. Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nat Genet. 2018 05; 50(5):668-681. Wray NR, Ripke S, Mattheisen M, Trzaskowski M, Byrne EM, Abdellaoui A, Adams MJ, Agerbo E, Air TM, Andlauer TMF, Bacanu SA, Bækvad-Hansen M, Beekman AFT, Bigdeli TB, Binder EB, Blackwood DRH, Bryois J, Buttenschøn HN, Bybjerg-Grauholm J, Cai N, Castelao E, Christensen JH, Clarke TK, Coleman JIR, Colodro-Conde L, Couvy-Duchesne B, Craddock N, Crawford GE, Crowley CA, Dashti HS, Davies G, Deary IJ, Degenhardt F, Derks EM, Direk N, Dolan CV, Dunn EC, Eley TC, Eriksson N, Escott-Price V, Kiadeh FHF, Finucane HK, Forstner AJ, Frank J, Gaspar HA, Gill M, Giusti-Rodríguez P, Goes FS, Gordon SD, Grove J, Hall LS, Hannon E, Hansen CS, Hansen TF, Herms S, Hickie IB, Hoffmann P, Homuth G, Horn C, Hottenga JJ, Hougaard DM, Hu M, Hyde CL, Ising M, Jansen R, Jin F, Jorgenson E, Knowles JA, Kohane IS, Kraft J, Kretzschmar WW, Krogh J, Kutalik Z, Lane JM, Li Y, Li Y, Lind PA, Liu X, Lu L, MacIntyre DJ, MacKinnon DF, Maier RM, Maier W, Marchini J, Mbarek H, McGrath P, McGuffin P, Medland SE, Mehta D, Middeldorp CM, Mihailov E, Milaneschi Y, Milani L, Mill J, Mondimore FM, Montgomery GW, Mostafavi S, Mullins N, Nauck M, Ng B, Nivard MG, Nyholt DR, O'Reilly PF, Oskarsson H, Owen MJ, Painter JN, Pedersen CB, Pedersen MG, Peterson RE, Pettersson E, Peyrot WJ, Pistis G, Posthuma D, Purcell SM, Quiroz JA, Qvist P, Rice JP, Riley BP, Rivera M, Saeed Mirza S, Saxena R, Schoevers R, Schulte EC, Shen L, Shi J, Shyn SI, Sigurdsson E, Sinnamon GBC, Smit JH, Smith DJ, Stefansson H, Steinberg S, Stockmeier CA, Streit F, Strohmaier J, Tansey KE, Teismann H, Teumer A, Thompson W, Thomson PA, Thorgeirsson TE, Tian C, Traylor M, Treutlein J, Trubetskoy V, Uitterlinden AG, Umbricht D, Van der Auwera S, van Hemert AM, Viktorin A, Visscher PM, Wang Y, Webb BT, Weinsheimer SM, Wellmann J, Willemsen G, Witt SH, Wu Y, Xi HS, Yang J, Zhang F, eQTLGen, 23andMe, Arolt V, Baune BT, Berger K, Boomsma DI, Cichon S, Dannlowski U, de Geus ECJ, DePaulo JR, Domenici E, Domschke K, Esko T, Grabe HJ, Hamilton SP, Hayward C, Heath AC, Hinds DA, Kendler KS, Kloiber S, Lewis G, Li QS, Lucae S, Madden PFA, Magnusson PK, Martin NG, McIntosh AM, Metspalu A, Mors O, Mortensen PB, Müller-Myhsok B, Nordentoft M, Nöthen MM, O'Donovan MC, Paciga SA, Pedersen NL, Penninx BWJH, Perlis RH, Porteous DJ, Potash JB, Preisig M, Rietschel M, Schaefer C, Schulze TG, Smoller JW, Stefansson K, Tiemeier H, Uher R, Völzke H, Weissman MM, Werge T, Winslow AR, Lewis CM, Levinson DF, Breen G, Børglum AD, Sullivan PF, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. PMID: 29700475; PMCID: PMC5934326.
      View in: PubMed   Mentions: 918     Fields:    Translation:Humans
    22. Abstract WP426: Does Intracerebral Hemorrhage in Brain Arteriovenous Malformation Share Genetic Risk Factors With Primary Intracerebral Hemorrhage?. Stroke. 2018 Jan 22; 49(Suppl_1). Nelson NJ, Bendjilali BN, Weinsheimer WS, McCulloch MC, Ko KN, Zaroff ZJ, Lawton LM, Pawlikowska PL, Kim KH. .
      View in: Publisher Site   Mentions:
    23. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome. Transl Psychiatry. 2017 08 29; 7(8):e1221. Starnawska A, Hansen CS, Sparsø T, Mazin W, Olsen L, Bertalan M, Buil A, Bybjerg-Grauholm J, Bækvad-Hansen M, Hougaard DM, Mortensen PB, Pedersen CB, Nyegaard M, Werge T, Weinsheimer S. PMID: 28850114; PMCID: PMC5611746.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    24. An epigenetic clock for gestational age at birth based on blood methylation data. Genome Biol. 2016 10 07; 17(1):206. Knight AK, Craig JM, Theda C, Bækvad-Hansen M, Bybjerg-Grauholm J, Hansen CS, Hollegaard MV, Hougaard DM, Mortensen PB, Weinsheimer SM, Werge TM, Brennan PA, Cubells JF, Newport DJ, Stowe ZN, Cheong JL, Dalach P, Doyle LW, Loke YJ, Baccarelli AA, Just AC, Wright RO, Téllez-Rojo MM, Svensson K, Trevisi L, Kennedy EM, Binder EB, Iurato S, Czamara D, Räikkönen K, Lahti JM, Pesonen AK, Kajantie E, Villa PM, Laivuori H, Hämäläinen E, Park HJ, Bailey LB, Parets SE, Kilaru V, Menon R, Horvath S, Bush NR, LeWinn KZ, Tylavsky FA, Conneely KN, Smith AK. PMID: 27717399; PMCID: PMC5054584.
      View in: PubMed   Mentions: 97     Fields:    Translation:HumansCells
    25. Genome-wide association study of sporadic brain arteriovenous malformations. J Neurol Neurosurg Psychiatry. 2016 09; 87(9):916-23. Weinsheimer S, Bendjilali N, Nelson J, Guo DE, Zaroff JG, Sidney S, McCulloch CE, Al-Shahi Salman R, Berg JN, Koeleman BP, Simon M, Bostroem A, Fontanella M, Sturiale CL, Pola R, Puca A, Lawton MT, Young WL, Pawlikowska L, Klijn CJ, Kim H, GEN-AVM Consortium. PMID: 26818729; PMCID: PMC4963303.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    26. Molecular basis and genetic predisposition to intracranial aneurysm. Ann Med. 2014 Dec; 46(8):597-606. Tromp G, Weinsheimer S, Ronkainen A, Kuivaniemi H. PMID: 25117779; PMCID: PMC4438354.
      View in: PubMed   Mentions: 40     Fields:    Translation:Humans
    27. Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain. J Neurol Neurosurg Psychiatry. 2015 May; 86(5):524-9. Kremer PH, Koeleman BP, Pawlikowska L, Weinsheimer S, Bendjilali N, Sidney S, Zaroff JG, Rinkel GJ, van den Berg LH, Ruigrok YM, de Kort GA, Veldink JH, Kim H, Klijn CJ. PMID: 25053769; PMCID: PMC4302044.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    28. Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms. J Neurol Neurosurg Psychiatry. 2014 Nov; 85(11):1280-3. Bendjilali N, Nelson J, Weinsheimer S, Sidney S, Zaroff JG, Hetts SW, Segal M, Pawlikowska L, McCulloch CE, Young WL, Kim H. PMID: 24777168; PMCID: PMC4201968.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    29. A genome-wide investigation of copy number variation in patients with sporadic brain arteriovenous malformation. PLoS One. 2013; 8(10):e71434. Bendjilali N, Kim H, Weinsheimer S, Guo DE, Kwok PY, Zaroff JG, Sidney S, Lawton MT, McCulloch CE, Koeleman BP, Klijn CJ, Young WL, Pawlikowska L. PMID: 24098321; PMCID: PMC3789669.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    30. Abstract TMP30: Genetic Variants on 9p21.3 are Associated with Brain Arteriovenous Malformations with Associated Arterial Aneurysms. Stroke. 2013 Feb 1; 44(suppl_1). Bendjilali BN, Nelson NJ, Weinsheimer WS, Sidney SS, Zaroff ZJ, Segal SM, Pawlikowska PL, McCulloch MC, Young YW, Kim KH. .
      View in: Publisher Site   Mentions:
    31. G Protein-Coupled Receptor 124 (GPR124) Gene Polymorphisms and Risk of Brain Arteriovenous Malformation. Transl Stroke Res. 2012 Dec; 3(4):418-27. Weinsheimer S, Brettman AD, Pawlikowska L, Wu DC, Mancuso MR, Kuhnert F, Lawton MT, Sidney S, Zaroff JG, McCulloch CE, Young WL, Kuo C, Kim H. PMID: 23329986; PMCID: PMC3544200.
      View in: PubMed   Mentions: 6     Fields:    
    32. Abstract 3666: Common Polymorphisms in Familial Vascular Malformation Genes do not Show Association with Sporadic Brain Arteriovenous Malformation. Stroke. 2012 Feb 1; 43(suppl_1). Weinsheimer WS, Bendjilali BN, Pawlikowska PL, Kwok KP, Lawton LM, Zaroff ZJ, Sidney SS, McCulloch MC, Kim KH, Young YW. .
      View in: Publisher Site   Mentions:
    33. Gene expression profiling of blood in brain arteriovenous malformation patients. Transl Stroke Res. 2011 Dec 01; 2(4):575-87. Weinsheimer SM, Xu H, Achrol AS, Stamova B, McCulloch CE, Pawlikowska L, Tian Y, Ko NU, Lawton MT, Steinberg GK, Chang SD, Jickling G, Ander BP, Kim H, Sharp FR, Young WL. PMID: 22184505; PMCID: PMC3241209.
      View in: PubMed   Mentions: 14     Fields:    
    34. Angiopoietin-like 4 (ANGPTL4) gene polymorphisms and risk of brain arteriovenous malformations. Cerebrovasc Dis. 2011; 31(4):338-45. Mikhak B, Weinsheimer S, Pawlikowska L, Poon A, Kwok PY, Lawton MT, Chen Y, Zaroff JG, Sidney S, McCulloch CE, Young WL, Kim H. PMID: 21212665; PMCID: PMC3030504.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    35. Brain arteriovenous malformation pathogenesis: a response-to-injury paradigm. Acta Neurochir Suppl. 2011; 111:83-92. Kim H, Su H, Weinsheimer S, Pawlikowska L, Young WL. PMID: 21725736; PMCID: PMC3187860.
      View in: PubMed   Mentions: 57     Fields:    Translation:HumansAnimals
    36. EPHB4 gene polymorphisms and risk of intracranial hemorrhage in patients with brain arteriovenous malformations. Circ Cardiovasc Genet. 2009 Oct; 2(5):476-82. Weinsheimer S, Kim H, Pawlikowska L, Chen Y, Lawton MT, Sidney S, Kwok PY, McCulloch CE, Young WL. PMID: 20031623; PMCID: PMC2939745.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    37. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 2008 Feb; 40(2):217-24. Helgadottir A, Thorleifsson G, Magnusson KP, Grétarsdottir S, Steinthorsdottir V, Manolescu A, Jones GT, Rinkel GJ, Blankensteijn JD, Ronkainen A, Jääskeläinen JE, Kyo Y, Lenk GM, Sakalihasan N, Kostulas K, Gottsäter A, Flex A, Stefansson H, Hansen T, Andersen G, Weinsheimer S, Borch-Johnsen K, Jorgensen T, Shah SH, Quyyumi AA, Granger CB, Reilly MP, Austin H, Levey AI, Vaccarino V, Palsdottir E, Walters GB, Jonsdottir T, Snorradottir S, Magnusdottir D, Gudmundsson G, Ferrell RE, Sveinbjornsdottir S, Hernesniemi J, Niemelä M, Limet R, Andersen K, Sigurdsson G, Benediktsson R, Verhoeven EL, Teijink JA, Grobbee DE, Rader DJ, Collier DA, Pedersen O, Pola R, Hillert J, Lindblad B, Valdimarsson EM, Magnadottir HB, Wijmenga C, Tromp G, Baas AF, Ruigrok YM, van Rij AM, Kuivaniemi H, Powell JT, Matthiasson SE, Gulcher JR, Thorgeirsson G, Kong A, Thorsteinsdottir U, Stefansson K. PMID: 18176561.
      View in: PubMed   Mentions: 305     Fields:    Translation:HumansCells
    38. Effects of cathepsins B and L inhibition on postischemic protein alterations in the brain. Biochem Biophys Res Commun. 2008 Feb 01; 366(1):86-91. Anagli J, Abounit K, Stemmer P, Han Y, Allred L, Weinsheimer S, Movsisyan A, Seyfried D. PMID: 18060871; PMCID: PMC3878606.
      View in: PubMed   Mentions: 14     Fields:    Translation:Animals
    39. Integration of expression profiles and genetic mapping data to identify candidate genes in intracranial aneurysm. Physiol Genomics. 2007 Dec 19; 32(1):45-57. Weinsheimer S, Lenk GM, van der Voet M, Land S, Ronkainen A, Alafuzoff I, Kuivaniemi H, Tromp G. PMID: 17878320.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    40. Association of kallikrein gene polymorphisms with intracranial aneurysms. Stroke. 2007 Oct; 38(10):2670-6. Weinsheimer S, Goddard KA, Parrado AR, Lu Q, Sinha M, Lebedeva ER, Ronkainen A, Niemelä M, Khusnutdinova EK, Khusainova RI, Helin K, Jääskeläinen JE, Sakovich VP, Land S, Kuivaniemi H, Tromp G. PMID: 17761919.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    41. Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms. BMC Genomics. 2007 Jul 16; 8:237. Lenk GM, Tromp G, Weinsheimer S, Gatalica Z, Berguer R, Kuivaniemi H. PMID: 17634102; PMCID: PMC1934369.
      View in: PubMed   Mentions: 72     Fields:    Translation:Humans
    42. LARALink: a web application for cytogenetic linkage analysis. Clin Genet. 2005 Apr; 67(4):314-21. Fayz B, Moldenhauer JS, Wang D, Zhao C, Yao B, Liu D, Weinsheimer S, Gardner L, Johnson A, Womble DD, Krawetz SA. PMID: 15733267.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    43. Structural determinants of the calpain inhibitory activity of calpastatin peptide B27-WT. J Biol Chem. 2003 Mar 07; 278(10):7800-9. Betts R, Weinsheimer S, Blouse GE, Anagli J. PMID: 12500971.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimalsCells
    44. A selective cysteine protease inhibitor is non-toxic and cerebroprotective in rats undergoing transient middle cerebral artery ischemia. Brain Res. 2001 May 18; 901(1-2):94-101. Seyfried DM, Veyna R, Han Y, Li K, Tang N, Betts RL, Weinsheimer S, Chopp M, Anagli J. PMID: 11368955.
      View in: PubMed   Mentions: 20     Fields:    Translation:AnimalsCells
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